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Imaging findings of mucopolysaccharidoses: a pictorial review
INTRODUCTION: Mucopolysaccharidosis (MPS) represent a heterogeneous group of inheritable lysosomal storage diseases in which the accumulation of undegraded glycosaminoglycans (GAGs) leads to progressive damage of affected tissues. The typical symptoms include organomegaly, dysostosis multiplex, ment...
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| Main Authors: | , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Springer Berlin Heidelberg
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3731470/ https://ncbi.nlm.nih.gov/pubmed/23645566 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13244-013-0246-8 |
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